Center for Research on Genomics and Global Health, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Hum Mol Genet. 2021 Apr 26;30(R1):R110-R118. doi: 10.1093/hmg/ddaa238.
Rates of type 2 diabetes (T2D) and hypertension are increasing rapidly in urbanizing sub-Saharan Africa (SSA). While lifestyle factors drive the increases in T2D and hypertension prevalence, evidence across populations shows that genetic variation, which is driven by evolutionary forces including a natural selection that shaped the human genome, also plays a role. Here we report the evidence for the effect of selection in African genomes on mechanisms underlying T2D and hypertension, including energy metabolism, adipose tissue biology, insulin action and salt retention. Selection effects found for variants in genes PPARA and TCF7L2 may have enabled Africans to respond to nutritional challenges by altering carbohydrate and lipid metabolism. Likewise, African-ancestry-specific characteristics of adipose tissue biology (low visceral adipose tissue [VAT], high intermuscular adipose tissue and a strong association between VAT and adiponectin) may have been selected for in response to nutritional and infectious disease challenges in the African environment. Evidence for selection effects on insulin action, including insulin resistance and secretion, has been found for several genes including MPHOSPH9, TMEM127, ZRANB3 and MC3R. These effects may have been historically adaptive in critical conditions, such as famine and inflammation. A strong correlation between hypertension susceptibility variants and latitude supports the hypothesis of selection for salt retention mechanisms in warm, humid climates. Nevertheless, adaptive genomics studies in African populations are scarce. More work is needed, particularly genomics studies covering the wide diversity of African populations in SSA and Africans in diaspora, as well as further functional assessment of established risk loci.
在城市化的撒哈拉以南非洲(SSA),2 型糖尿病(T2D)和高血压的发病率正在迅速上升。虽然生活方式因素导致了 T2D 和高血压患病率的增加,但来自不同人群的证据表明,遗传变异也发挥了作用,而遗传变异是由进化力量驱动的,包括塑造人类基因组的自然选择。在这里,我们报告了选择对非洲基因组中与 T2D 和高血压相关机制的影响的证据,包括能量代谢、脂肪组织生物学、胰岛素作用和盐潴留。在 PPARA 和 TCF7L2 基因中的变异发现的选择效应可能使非洲人能够通过改变碳水化合物和脂质代谢来应对营养挑战。同样,脂肪组织生物学(低内脏脂肪组织[VAT]、高肌肉间脂肪组织和 VAT 与脂联素之间的强烈关联)的非洲人特有的特征可能是为了应对非洲环境中的营养和传染病挑战而选择的。在包括胰岛素抵抗和分泌在内的胰岛素作用方面,已经发现了几个基因(包括 MPHOSPH9、TMEM127、ZRANB3 和 MC3R)的选择效应。这些影响在饥荒和炎症等关键条件下可能具有历史适应性。高血压易感性变异与纬度之间的强烈相关性支持了在温暖潮湿气候中选择盐潴留机制的假说。然而,非洲人群中的适应性基因组学研究仍然很少。需要做更多的工作,特别是涵盖 SSA 中的非洲人群和散居海外的非洲人以及对已建立的风险基因座进行进一步功能评估的基因组学研究。